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Biodegradable Stenting Anastomoses Versus Double-layer Hand Sutures for Reconstruction in Intestinal Anastomosis

Biodegradable Stenting Anastomoses Versus Double-layer Hand Sutures for Reconstruction in Surgery of Intestinal Anastomosis: A Multicenter, Prospective Cohort Study

Status
UNKNOWN
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02752360
Enrollment
288
Registered
2016-04-27
Start date
2016-04-30
Completion date
2018-12-31
Last updated
2017-06-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colonic Neoplasms, Crohn Disease, Diverticulosis, Colonic

Keywords

intestinal reconstruction, end to end anastomosis

Brief summary

Intestinal anastomosis plays an important role in various general surgeries, but the complications such as anastomotic leakage,stenosis and hemorrhage cannot been avoided. Although many ways are put up to solve this problem, there are still many imports need to improve. Therefore, the Biodegradable Stenting Anastomoses(BSA), which make intestinal anastomosis easily and less complications, have been produced.The major goal of this study is to evaluate the efficacy of Biodegradable Stenting Anastomoses(BSA) for reconstruction in surgery of intestinal anastomosis.

Interventions

PROCEDUREBiodegradable Stenting Anastomoses

Biodegradable Stenting Anastomoses(BSA) is a new method and device which helps to make intestinal anastomosis easily. According to the measurement of intestinal canal diameter, chose an appropriate size of BSA and use the Seromuscular layer Purse-string Suture to stitch with an absorbable line (VCP311, Ethicon, Inc.) away from the end 0.5 to 1.0 cm and not knot temporarily, then open and sterilize intestinal canal fully, and place the BSA into the intestinal canal at appropriate position before tightening knot. Last, the interrupted whole layer inversion suture is used to fix.

PROCEDUREDouble-layer Hand Sutures

Double-layer Hand Sutures(DHS)is a surgery way that is to use the single-layer continous Hand Sutures,then Lembert to stitch with an absorbable line (VCP311, Ethicon, Inc.).

Sponsors

Peking University Third Hospital
CollaboratorOTHER
Zhejiang Cancer Hospital
CollaboratorOTHER
Beijing Friendship Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with age between 18 - 80 years. * Patients with operation of end to end anastomosis of colon or small intestine. * Patients without previous surgery during 3 months. * Patients who understand the nature of this trial and provide informed consent.

Exclusion criteria

* Patients with severe cardiopulmonary disease or other severe disease. * Patients who are psychopath, pregnant, and child without capacity for civil conduct. * Patients with complete intestinal obstruction. * Patients with abdominal cavity infection. * Patients who are treating by drug such as adrenal cortical hormone and immune inhibitors, chemotherapy drugs, radiation and so on. * Patients who need to accept the anastomosis between rectum and colon. * Patients who are required to accept intestinal anastomosis twice or more. * Patients who are required to accept the treatment of colostomy. * other conditions that render a patient unsuitable for the trial as determined by the study investigators.

Design outcomes

Primary

MeasureTime frameDescription
Anastomotic Leakage Rate7-10 DaysThe patients with anastomotic leakage / the total patients. The definition of anastomotic leakage in this study, is included one of the situation as follows: (1) peritonitis caused by leakage, pelvic abscess without radiologically proven anastomotic leakage were considered as equivalents of clinically anastomotic leakage as defined above.; (2) Discharge of faeces, pus or gas from the abdominal drain; (3) All anastomotic leakages were confirmed by one or more of the following methods such as CT scan, ultrasonography and laparotomy.
Anastomotic Hemorrhage Rate2 WeeksThe patients with anastomotic hemorrhage / the total patients. Anastomotic bleeding was considered gastrointestinal bleeding after surgery, and it ascertains that the bleeding is from anastomosis with endoscopy.
Anastomotic Stenosis Rate6 MonthsThe patients with anastomotic stenosis / the total patients.Anastomotic stenosis which is not caused by tumor in the patients with complete or incomplete intestinal obstruction symptoms.

Secondary

MeasureTime frameDescription
Number of participant with abnormal laboratory values6 MonthsNumber of participant with abnormal laboratory values will be record. Laboratory tests include Blood routine/Coagulation/Liver and renal function/Electrolyte/Lipids/OB. Abnormal laboratory values means that values of Laboratory tests beyond the normal values.
The time of reconstruction in the surgery of Intestinal Anastomosis1 DayThe time of reconstruction in the surgery of Intestinal Anastomosis for each group is recorded, which is from the beginning to the ending of Intestinal Anastomosis
Severe adverse events (SAEs)6 MonthsSevere adverse events (SAEs) refer to the following conditions: death, life-threatening or permanent or significant disability, permanent functional injury to the organs, hospitalization for emergencies or prolonged hospitalization
Whether the Biodegradable Stenting Anastomoses be eliminated or not6 MonthsThe enteroscopy will be used to observe whether the Biodegradable Stenting Anastomoses be eliminated from body at 4th weeks after surgery.If Biodegradable Stenting Anastomoses be eliminated, contrast will be filling defect.

Countries

China

Contacts

Primary ContactGuocong Wu, Doctor
dr.wuguocong@qq.com+86 13810354857

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026